510(k) K931169

MDT DENTAL CHAIR by Mdt Corp., Inc. — Product Code KLC

K931169 is an FDA 510(k) premarket notification submitted by Mdt Corp., Inc. for the device "MDT DENTAL CHAIR". The FDA issued a decision of Substantially Equivalent on May 20, 1993. The device falls under product code KLC (Chair, Dental, With Operative Unit), a Class I device regulated under 21 CFR 872.6250. Mdt Corp., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 20, 1993
Date Received
March 8, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Chair, Dental, With Operative Unit
Device Class
Class I
Regulation Number
872.6250
Review Panel
DE
Submission Type